Sporadic rapid-onset dystonia-parkinsonism syndrome:: Failure of bilateral pallidal stimulation
Sporadic rapid-onset dystonia-parkinsonism syndrome:: Failure of bilateral pallidal stimulation
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DOI：
10.1002/mds.20296
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发表时间：
2005-02-01
影响因子：
8.6
通讯作者：
Bötzel, K
中科院分区：
文献类型：
--
作者：
Deutschländer, A;Asmus, F;Bötzel, K
我们报告了一名21岁的女性，她患有严重的散发性非进行性肌张力障碍-帕金森综合征，症状发作迅速。排除了肌张力障碍的继发原因。左旋多巴/卡比多巴无反应。除常染色体显性遗传外，患者符合所有快速发作性肌张力障碍-帕金森病的诊断标准。双侧脑深部刺激苍白球未能缓解她的症状。(C) 2004运动障碍学会。
We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms. (C) 2004 Movement Disorder Society.